Canonical Allele Identifier: CA2499221756
Gene: ITGA7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.55695572_55695573delinsAT , CM000674.2:g.55695572_55695573delinsAT GRCh38
NC_000012.11:g.56089356_56089357delinsAT , CM000674.1:g.56089356_56089357delinsAT GRCh37
NC_000012.10:g.54375623_54375624delinsAT NCBI36
NG_012343.1:g.21733_21734delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000553893.6:c.*1576_*1577delinsAT ENSP00000452467.1:n.*1576_*1577delinsAT
ENST00000554327.6:c.816_817delinsAT
ENST00000557058.2:n.816_817delinsAT
ENST00000557257.2:c.1478_1479delinsAT ENSP00000450578.2:p.Arg493His
ENST00000557555.3:c.1964_1965delinsAT ENSP00000451039.3:p.Arg655His
ENST00000686981.1:c.*1663_*1664delinsAT ENSP00000510795.1:n.*1663_*1664delinsAT
ENST00000691052.1:c.*436_*437delinsAT ENSP00000508886.1:n.*436_*437delinsAT
ENST00000691846.1:c.797_798delinsAT
ENST00000691973.1:c.1964_1965delinsAT ENSP00000509141.1:p.Arg655His
ENST00000257879.11:c.1952_1953delinsAT MANE Select ENSP00000257879.7:p.Arg651His
ENST00000553804.6:c.1964_1965delinsAT ENSP00000452120.1:p.Arg655His
ENST00000257879.10:c.1952_1953delinsAT ENSP00000257879.6:p.Arg651His
ENST00000347027.10:c.1934_1935delinsAT ENSP00000343009.6:p.Arg645His
ENST00000452168.6:c.1673_1674delinsAT ENSP00000393844.2:p.Arg558His
ENST00000553804.5:c.1964_1965delinsAT ENSP00000452120.1:p.Arg655His
ENST00000554327.5:c.210_211delinsAT
ENST00000555728.5:c.2084_2085delinsAT ENSP00000452387.1:p.Arg695His
ENST00000557058.1:n.199_200delinsAT
NM_001144996.1:c.1964_1965delinsAT NP_001138468.1:p.Arg655His
NM_001144997.1:c.1673_1674delinsAT NP_001138469.1:p.Arg558His
NM_002206.2:c.1952_1953delinsAT NP_002197.2:p.Arg651His
XM_005268839.1:c.2084_2085delinsAT XP_005268896.1:p.Arg695His
XM_005268840.1:c.2066_2067delinsAT XP_005268897.1:p.Arg689His
XM_005268841.1:c.2084_2085delinsAT XP_005268898.1:p.Arg695His
XM_005268842.1:c.1934_1935delinsAT XP_005268899.1:p.Arg645His
XM_005268844.1:c.1745_1746delinsAT XP_005268901.1:p.Arg582His
XM_005268845.1:c.1613_1614delinsAT XP_005268902.1:p.Arg538His
XM_005268846.1:c.1613_1614delinsAT XP_005268903.1:p.Arg538His
XM_005268847.1:c.1610_1611delinsAT XP_005268904.1:p.Arg537His
XM_005268848.1:c.1610_1611delinsAT XP_005268905.1:p.Arg537His
XM_005268849.1:c.1610_1611delinsAT XP_005268906.1:p.Arg537His
XM_005268850.1:c.1478_1479delinsAT XP_005268907.1:p.Arg493His
XM_011538286.1:c.1745_1746delinsAT XP_011536588.1:p.Arg582His
XM_011538287.1:c.2084_2085delinsAT XP_011536589.1:p.Arg695His
XM_005268839.2:c.2084_2085delinsAT XP_005268896.1:p.Arg695His
XM_005268840.2:c.2066_2067delinsAT XP_005268897.1:p.Arg689His
XM_005268841.2:c.2084_2085delinsAT XP_005268898.1:p.Arg695His
XM_005268842.2:c.1934_1935delinsAT XP_005268899.1:p.Arg645His
XM_017019265.1:c.1694_1695delinsAT XP_016874754.1:p.Arg565His
NM_001144996.2:c.1964_1965delinsAT NP_001138468.1:p.Arg655His
NM_001367993.1:c.1625_1626delinsAT NP_001354922.1:p.Arg542His
NM_001367994.1:c.608_609delinsAT NP_001354923.1:p.Arg203His
NM_001374465.1:c.1934_1935delinsAT NP_001361394.1:p.Arg645His
NM_002206.3:c.1952_1953delinsAT MANE Select NP_002197.2:p.Arg651His